Venkateswaran Nandini, Yeaney Gabrielle, Chung Mina, Hindman Holly B
University of Rochester School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA.
Department of Pathology and Laboratory Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Clin Ophthalmol. 2014 May 2;8:837-42. doi: 10.2147/OPTH.S56670. eCollection 2014.
To report a case of recurrent nontuberculous mycobacterial endophthalmitis in the context of neurotrophic keratopathy secondary to herpes zoster ophthalmicus that had an atypical presentation and complex course, and highlights the challenges of causative organism identification and therapeutic interventions in this condition.
A retrospective chart review was conducted to determine the visual outcomes of the patient.
A 68-year-old pseudophakic male with long-standing neurotrophic keratopathy and perforated descemetocele managed with cyanoacrylate glue and a contact bandage lens in the left eye, began experiencing recurrent episodes of endophthalmitis after undergoing a penetrating keratoplasty. Several therapeutic procedures including an anterior chamber washout, two pars plana vitrectomies, explantation of the posterior chamber intraocular lens and capsular bag, and multiple intravitreal antimicrobial injections, were performed to which he has ultimately responded favorably, with no signs of infection to date and stable visual acuity. The causative organism of his recurrent infections was initially identified as Mycobacterium abscessus through biochemical testing and 16S ribosomal ribonucleic acid gene sequencing; however, repeat polymerase chain reaction (PCR) and sequencing of the 65 kDa heat shock protein (hsp65) gene for experimental purposes confirmed the accurate identification of the organism to be Mycobacterium chelonae. Given the greater reliability of PCR and sequencing of the hsp65 gene over traditional biochemical tests and culture techniques, M. chelonae was likely the infectious agent all along, and the organism was originally misidentified on the basis of less accurate tests.
Recurrent atypical mycobacterial endophthalmitis requires expedient identification and management to prevent poor visual outcomes. Standard biochemical testing can identify the causative organism but is limited by the inability to distinguish between nontuberculous species reliably. We recommend the use of PCR in conjunction with sequencing of the hsp65 gene for reliable differentiation of M. chelonae and M. abscessus in atypical mycobacterial ocular infections. Minimum inhibitory concentration antibiotic susceptibility tests on cultured strains are the best guide to antibiotic selection, given the rapidly rising resistance to antimicrobials in atypical mycobacterial species.
报告1例继发于眼部带状疱疹的神经营养性角膜病变患者发生的复发性非结核分枝杆菌性眼内炎,该病例表现不典型且病程复杂,并强调在这种情况下确定病原体及进行治疗干预所面临的挑战。
进行回顾性病历审查以确定患者的视力预后。
一名68岁的假晶状体男性,左眼长期患有神经营养性角膜病变且存在穿孔性后弹力层膨出,曾用氰基丙烯酸酯胶水和接触绷带镜进行处理,在接受穿透性角膜移植术后开始出现复发性眼内炎。进行了包括前房冲洗、两次玻璃体切割术、取出后房型人工晶状体和囊袋以及多次玻璃体内抗微生物注射在内的多种治疗措施,患者最终反应良好,迄今无感染迹象且视力稳定。通过生化检测和16S核糖体核糖核酸基因测序,其复发性感染的病原体最初被鉴定为脓肿分枝杆菌;然而,出于实验目的对65 kDa热休克蛋白(hsp65)基因进行的重复聚合酶链反应(PCR)和测序证实,该病原体准确鉴定为龟分枝杆菌。鉴于hsp65基因的PCR和测序比传统生化检测和培养技术具有更高的可靠性。龟分枝杆菌很可能一直是感染源,最初是基于不太准确的检测而被错误鉴定。
复发性非典型分枝杆菌性眼内炎需要及时识别和处理,以防止视力预后不良。标准生化检测可确定病原体,但受限于无法可靠地区分非结核分枝杆菌种类。我们建议在非典型分枝杆菌性眼部感染中联合使用PCR和hsp65基因测序,以可靠地区分龟分枝杆菌和脓肿分枝杆菌。鉴于非典型分枝杆菌对抗微生物药物的耐药性迅速上升,对培养菌株进行最低抑菌浓度抗生素敏感性试验是抗生素选择的最佳指导。